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EP2708531A1 - Formes Cristallines De 3-[5-Chloro-4-(2,4-difluorobenzyl) oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide - Google Patents

Formes Cristallines De 3-[5-Chloro-4-(2,4-difluorobenzyl) oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide Download PDF

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Publication number
EP2708531A1
EP2708531A1 EP13186682.4A EP13186682A EP2708531A1 EP 2708531 A1 EP2708531 A1 EP 2708531A1 EP 13186682 A EP13186682 A EP 13186682A EP 2708531 A1 EP2708531 A1 EP 2708531A1
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EP
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Prior art keywords
compound
oxopyrimidin
difluorobenzyl
oxy
chloro
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Withdrawn
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EP13186682.4A
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German (de)
English (en)
Inventor
Jon G Selbo
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Pharmacia and Upjohn Co LLC
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Pharmacia and Upjohn Co LLC
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Publication of EP2708531A1 publication Critical patent/EP2708531A1/fr
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Definitions

  • This invention is in the field of pharmaceutical agents active as p38 kinase inhibitors, and more particularly concerns the p38 kinase inhibitor 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide.
  • the invention relates to a novel forms of 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide.
  • Compound 1 The compound 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide having the structure (1) below (referred to herein as "Compound 1") is described in US patent application No.10/808,146 (filed 3/24/2004 ) discloses a class of substituted pyrimidinone compounds and related pharmaceutical compositions that are useful for the treatment and/or prophylaxis of a p38 kinase-mediated condition, example of such include inflammation and inflammation related conditions.
  • novel crystalline forms of Compound 1 having a high degree of physical stability at common temperatures of storage and use.
  • the invention provides, in a first aspect, an anhydrous crystalline form of Compound 1 ("Form A").
  • the invention provides pharmaceutical compositions comprising Form A, and further optionally comprising one or more pharmaceutically acceptable excipients.
  • the invention provides pharmaceutical compositions containing about 0.1 mg to about 1000 mg of Form A.
  • the invention provides a method for prophylaxis and/or treatment of an inflammatory condition comprising administering to a subject a therapeutically effective amount of Form A.
  • the invention provides, in a second aspect, a hydrous crystalline form of Compound 1 ("Form B").
  • the invention provides pharmaceutical compositions comprising Form B, and further optionally comprising one or more pharmaceutically acceptable excipients.
  • the invention provides pharmaceutical compositions containing about 0.1 mg to about 1000 mg of Form B.
  • the invention provides a method for prophylaxis and/or treatment of an inflammatory condition comprising administering to a subject a therapeutically effective amount of Form B.
  • Figure 1 shows an illustrative X-ray powder diffraction pattern for Form A.
  • Figure 2 shows an illustrative X-ray powder diffraction pattern for Form B.
  • Figure 3 shows an illustrative X-ray powder diffraction pattern for Form C.
  • Figure 4 shows an illustrative differential scanning calorimetry thermogram of Form A.
  • Figure 5 shows an illustrative differential scanning calorimetry thermogram of Form C.
  • Figure 6 shows an illustrative Thermogravimetric Analysis of Form A.
  • Figure 7 shows an illustrative Thermogravimetric Analysis of Form C.
  • Figure 8 shows an illustrative infrared (IR) spectrum of Form B.
  • Figure 9 shows an illustrative Raman spectrum of Form A.
  • Figure 10 shows an illustrative Raman spectrum of Form B.
  • Figure 11 shows an illustrative DVS of Form A.
  • Figure 12 shows an illustrative DVS of Form B.
  • Figure 13 shows an illustrative DVS of Form C.
  • the present invention relates to crystalline forms of 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide.
  • Polymorphs are different crystalline forms of the same compound. Different crystalline forms can have different physical properties such as different melting point, powder x-ray and solid state NMR.
  • the present invention relates to three different crystalline forms of 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide.
  • the present invention provides an anhydrous crystalline form of Compound 1("Form A").
  • the invention provides, in a second aspect, a hydrous crystalline form of Compound 1("Form B").
  • the invention provides, in a third aspect, a hydrous crystalline form of Compound 1("Form C").
  • These properties include, but are not limited to: (1) packing properties such as molar volume, density and hygroscopicity, (2) thermodynamic properties such as melting temperature, vapor pressure and solubility, (3) kinetic properties such as dissolution rate and stability (including stability at ambient conditions, especially to moisture, and under storage conditions), (4) surface properties such as surface area, wettability, interfacial tension and shape, (5) mechanical properties such as hardness, tensile strength, compactibility, handling, flow and blend, (6) filtration properties, (7) chemical purity, and (8) physical and chemical stability. These properties can affect, for example, processing and storage of pharmaceutical compositions comprising Compound 1. Solid-state forms of Compound 1 that provide an improvement in one or more of these properties relative to other solid-state forms of Compound 1 are desirable.
  • the specific solid-state form of Compound 1 includes an anhydrous crystalline form possessing thermodynamic stability under normal manufacturing conditions.
  • the invention comprises the Form A of Compound 1.
  • the Form A possesses physical stability at ambient temperatures. Solid-state forms of Compound 1 that do not require special processing or storage conditions, and that avoid the need for frequent inventory replacement, such as Form A, are desirable. For example, selection of a solid-state form of Compound 1 that is physically stable during a manufacturing process (such as during milling of Compound 1 to obtain a material with reduced particle size and increased surface area) can avoid the need for special processing conditions and the increased costs generally associated with such special processing conditions.
  • selection of a solid-state form of Compound 1 that is physically stable over a wide range of storage conditions can help avoid polymorphic or other degradative changes in the Compound 1 that can lead to product loss or deterioration of product efficacy. Therefore, the selection of a solid-state form of Compound 1 such as Form A having greater physical stability provides a meaningful benefit over less stable Compound 1 solid-state forms.
  • the solid-state form of Compound 1 described in this application is useful for, but not limited to, the treatment of any condition in a human, or other mammal, which is exacerbated or caused by excessive or unregulated cytokine production by the mammal, such as TNF or p38 kinase production.
  • the solid-state forms of Compound 1 is p38 kinase antagonists, directly or indirectly antagonize cytokines such as TNF and IL-1 proteins, and/or have the ability to retard the natural course of joint destruction in rheumatoid arthritis patients. Accordingly, the present invention provides a method of treating a cytokine-mediated condition, which comprises administering to a subject an effective cytokine-interfering amount of a solid-state form of Compound 1.
  • Compound 1 is useful for, but not limited to, the treatment or prophylaxis of:
  • the crystalline form of Compound 1 disclosed in this application is also useful for preventing the production or expression of cyclooxygenase-2, or cyclooxygenase-2 activity.
  • crystalline form refers to a solid-state form wherein the Compound 1 molecules are arranged to form a distinguishable crystal lattice (i) comprising distinguishable unit cells, and (ii) yielding diffraction peaks when subjected to X-ray radiation.
  • crystallization can refer to crystallization and/or recrystallization depending upon the applicable circumstances relating to preparation of Compound 1 starting material.
  • direct crystallization refers to crystallization of Compound 1directly from a suitable solvent without formation and desolvation of an intermediate solvated crystalline solid-state form of Compound 1.
  • Compound 1 drug substance means Compound 1 per se as qualified by the context in which the term is used, and can refer to unformulated Compound 1or to Compound 1present as an ingredient of a pharmaceutical composition.
  • particle size refers to particle size as measured by conventional particle size measuring techniques well known in the art, such as laser light scattering, sedimentation field flow fractionation, photon correlation spectroscopy or disk centrifugation.
  • particle size is a technique that can be used to measure particle size.
  • D 90 particle size is a particle size such that 90% by weight of the particles are smaller than the D 90 particle size as measured by such conventional particle size measuring techniques.
  • DSC differential scanning calorimetry
  • HPLC means high pressure liquid chromatography
  • IR means infrared
  • purity herein, unless otherwise qualified, means the chemical purity of Compound 1 according to conventional HPLC assay.
  • phase purity herein means the solid-state purity of Compound 1with regard to a particular crystalline or amorphous form of the Compound 1 as determined by X-ray powder diffraction analytical methods described herein.
  • phase pure refers to purity with respect to other solid-state forms of Compound 1 and does not necessarily imply a high degree of chemical purity with respect to other compounds.
  • PXRD means X-ray powder diffraction
  • TGA thermogravimetric analysis
  • Powder X-ray Diffraction was performed using a Bruker D-8 Advance diffractometer (serial #002096) operating under DIFFRACplus 2000 and Microsoft Windows NTTM 4.0 software.
  • the system used a copper X-ray source maintained at 40 kV and 40 mA to provide Cu K ⁇ 1 (1.5406 ⁇ ) and Cu K ⁇ 2 (1.54439 A) radiation with an intensity weighted average of (K ⁇ ave ) 1.54184 ⁇ .
  • a scintillation counter was used for detection.
  • Beam aperture was controlled using primary 2° Soller slits and a fixed divergence slit of 2 mm.
  • a diffracted beam monochromator was used to remove K ⁇ radiation and fixed 2 mm anti-scatter, secondary 2° Soller slits, 0.2 mm monochromator, and 0.6 mm detector slits were employed. Data were collected using a step scan of 0.02° per point with a 0.1 second/point counting time over a range of 3 to 35° two-theta.
  • Bruker Round, top loading, stainless steel sample cups or fabricated aluminum inserts held in Bruker plastic sample cup holders were utilized for all analyses. Samples were run as is or after light hand grinding.
  • Table 1 presents data obtained for a sample of Form A.
  • Table 1 X-Ray Diffraction Data Angle (2-theta degrees) d-value Intensity (Counts) Intensity (%) 6.74 13.111 78 18.7 10.38 8.515 214 51.2 10.59 8.347 88 21.1 11.34 7.799 63 15.1 13.49 6.559 344 82.3 15.2 5.825 27 6.5 15.51 5.708 87 20.8 15.78 5.611 95 22.7 16.18 5.473 170 40.7 17.58 5.041 299 71.5 17.68 5.013 297 71 18.11 4.893 275 65.8 18.47 4.799 46 11 19.46 4.557 40 9.6 20.3 4.371 248 59.3 20.73 4.281 238 56.9 21.08 4.21 385 92.1 21.9 4.055 193 46.2 22.76 3.904 345 82.5 23.76 3.742 77 18.4 24.48 3.634 57 13.6 24.8 3.587 40 9.6 25.43
  • Form A typically has an X-ray powder diffraction pattern comprising at least one peak selected from the group consisting of 13.5 ⁇ 0.2, 17.6 ⁇ 0.2, 17.7 ⁇ 0.2, 21.1 ⁇ 0.2, 22.8 ⁇ 0.2, 25.4 ⁇ 0.2, and 27.2 ⁇ 0.2 degrees 2 theta.
  • the solid-state form of Compound 1 is Form A having an X-ray powder diffraction pattern comprising peaks at 13.5 ⁇ 0.2, 21.1 ⁇ 0.2, 22.8 ⁇ 0.2, 25.4 ⁇ 0.2 and 27.2 ⁇ 0.2 degrees 2 theta.
  • the solid-state form of Compound 1 is Form A having an X-ray powder diffraction pattern comprising peaks at 13.5 ⁇ 0.2, 21.1 ⁇ 0.2 and 27.2 ⁇ 0.2 degrees 2 theta.
  • Figure 1 shows an illustrative X-ray powder diffraction pattern for Form A.
  • Table 2 presents data obtained for a sample of Form B.
  • Table 2 X-Ray Diffraction Data Angle (2-theta degrees) d-value Intensity (Counts) Intensity (%) 5.56 15.891 84 24.1 6.85 12.898 101 28.9 7.94 11.129 53 15.2 11.08 7.982 65 18.6 11.81 7.486 231 66.2 13.68 6.467 165 47.3 14.08 6.286 26 7.4 15.81 5.602 169 48.4 16.65 5.32 66 18.9 18.51 4.789 43 12.3 19.15 4.63 110 31.5 20.18 4.397 79 22.6 20.97 4.232 61 17.5 21.38 4.153 151 43.3 21.89 4.056 134 38.4 22.22 3.998 105 30.1 22.69 3.915 66 18.9 23.21 3.828 81 23.2 23.67 3.756 106 30.4 24.41 3.644 107 30.7 25.2 3.532 78 22.3 26.23 3.395 112 32.1 26.89
  • Form B typically has an X-ray powder diffraction pattern comprising at least one peak selected from the group consisting of 11.8 ⁇ 0.2, 13.7 ⁇ 0.2, 15.8 ⁇ 0.2, 21.4 ⁇ 0.2, 21.9 ⁇ 0.2, 26.2 ⁇ 0.2, and 26.9 ⁇ 0.2 degrees 2 theta.
  • the solid-state form of Compound 1 is Form B having an X-ray powder diffraction pattern comprising peaks at 11.8 ⁇ 0.2, 13.7 ⁇ 0.2, 15.8 ⁇ 0.2, 21.4 ⁇ 0.2 and 26.9 ⁇ 0.2 degrees 2 theta.
  • the solid-state form of Compound 1 is Form B having an X-ray powder diffraction pattern comprising peaks at 11.8 ⁇ 0.2, 15.8 ⁇ 0.2 and 26.9 ⁇ 0.2 degrees 2 theta.
  • Figure 2 shows an illustrative X-ray powder diffraction pattern for Form B.
  • Table 3 presents data obtained for a sample of Form C.
  • Table 3 X-Ray Diffraction Data Angle (2-theta degrees) d-value Intensity (Counts) Intensity (%) 3.87 22.809 219 40.9 7.71 11.463 106 19.8 8.03 11.005 535 100 10.4 8.496 47 8.8 13.51 6.547 47 8.8 14.61 6.06 91 17 15.36 5.762 299 55.9 16.06 5.515 137 25.6 16.91 5.238 167 31.2 18.18 4.874 46 8.6 19.21 4.617 81 15.1 21.55 4.12 174 32.5 22.52 3.944 94 17.6 23.1 3.847 40 7.5 24.49 3.631 120 22.4 25.15 3.538 111 20.7 26.25 3.392 99 18.5 27.03 3.296 99 18.5 28.36 3.144 219 40.9 28.62 3.117 115 21.5 29.42 3.033 70 13.1 30.64 2.915 72 13.5 31.59 2.83 54 10.1
  • Figure 3 shows an illustrative X-ray powder diffraction pattern for Form C.
  • a Mettler DSC822e heat flux differential scanning calorimeter (S/N 515) was used to collect the heat flow versus temperature data for the set of experiments.
  • the samples were sealed in high-pressure gold-coated stainless steel (Au/SS) capsules for the experiments discussed in this report.
  • a Julabo intercooler was used to maintain temperature control of this instrument. Dry nitrogen at 60 cc/min was used as the purge gas. Samples were heated at 3°C/min from 20°C to 200°C.
  • the Mettler Star software for Windows NT was used to collect the signal and analyze the data. The temperature and heat flow axis were calibrated using indium.
  • Figure 4 shows an illustrative differential scanning calorimetry thermogram of Form A.
  • Figure 5 shows an illustrative differential scanning calorimetry thermogram of Form C.
  • DSC can also be used to characterize Form B.
  • thermogravimetric analyzer simultaneous differential thermal analyzer (S/N 286) was used to collect the weight loss and sample temperature versus temperature data.
  • the samples were sealed in 40uL pierceable aluminum capsules.
  • the instrument robot was used to pierce the samples before insertion into the furnace.
  • a Julabo circulator was used to maintain temperature control of this instrument.
  • Dry nitrogen at 50 cc/min was used as the purge gas.
  • Samples were heated at 5°C/min from 20°C to 400°C.
  • the Mettler Star software for Windows NT was used to collect the signal and analyze the data.
  • the temperature and simulated heat flow axis were calibrated using indium.
  • Figure 6 shows an illustrative Thermogravimetric Analysis of Form A.
  • Figure 7 shows an illustrative Thermogravimetric Analysis of Form C.
  • Thermogravimetric Analysis can also be used to characterize Form B.
  • Infrared Spectroscopy was done on a Thermo-Nicolet Corporation Nexus 670 FT-IR using an Avatar Ge ATR Omni-Sampler. Up to 64 scans with a 4 cm -1 resolution were averaged to reduce noise. A KBr beamsplitter and a MCT/A detector were employed.
  • Table 4 presents data obtained for a sample of Form A.
  • Table 4 Position Intensity 1070.37 0.196 773.03 0.153 1503.92 0.146 1640.83 0.14 1655.18 0.137 960.15 0.122 805.24 0.117 1330.79 0.109 1311.43 0.108 1462.76 0.105 1094.36 0.103 1514.67 0.102 870.28 0.0998 1276.64 0.0939 1593.56 0.0913 1545.85 0.083 969.8 0.0828 1139 0.0803 1221.84 0.0777 1418.17 0.0777 723.97 0.0751 750.18 0.0685 1568.53 0.0631 1384.13 0.0503 1199.82 0.0456 1251.67 0.041 924.16 0.0391 691.81 0.0385 3362.38 0.0344 712.22 0.0294 846.67 0.0289
  • Table 5 presents data obtained for a sample of Form B.
  • Table 5 Position Intensity 1661.08 0.117 1079.48 0.0586 1331.71 0.0551 1068.84 0.0496 1439.27 0.0434 1641.82 0.0409 1426.43 0.0328 1509.71 0.0299 1246.63 0.0294 1549.33 0.0286 1268.15 0.0254 1596.06 0.0213 1558.33 0.0186 1457.12 0.0178 1373.24 0.0161 962.65 0.0134 1092.33 0.0125 1618.08 0.0104 1575.82 0.0079 3346.22 0.0062 1683.99 0.0053 887.48 0.0045 1142.82 0.0023 1384 0.0019 3653.34 0.0014 1700.49 0.0011 3048.87 -0.0046 1185.05 -0.0046 1044.46 -0.0064 926.78 -0.008 1718.15 -0.0097
  • Figure 8 shows an illustrative infrared (IR) spectrum of Form B.
  • Raman spectra were obtained on a FT-Raman module with a FT-Raman micro view stage.
  • the FT-Raman module was attached to the Nexus 670 Bench.
  • a CaF 2 beamsplitter and a Ge detector were used. Up to 128 scans with a resolution of 2 cm -1 were done on each sample. Both instruments were controlled by Omnic 6.0A software. Atlus mapping 6.0 software was used to control the Raman view stage.
  • Table 6 presents data obtained for a sample of Form A.
  • Table 6 Position Intensity 1616.87 5.411 3076.75 5.193 1515.08 5.004 832.65 4.815 1310.32 3.871 1331.95 3.596 661.95 3.363 1301.64 3.187 2927.48 3.116 1273.48 3.1 1251.69 2.994 725.58 2.829 1638.1 2.756 2966.89 2.552 1455.18 2.457 1284.12 2.366 1417.57 2.35 785.78 2.338 1426.06 2.223 581.69 2.23 1666.31 2.073 1549.95 1.998 969.66 1.982 926.48 1.916 751.68 1.728 891.22 1.672 2998.34 1.649 2905.82 1.581 493.36 1.585 1376.98 1.504 1463.55 1.465 1568.51 1.391 1051.15 1.38 1385.12 1.364 1095 1.313 455.15 1.2
  • Table 7 presents data obtained for a sample of Form B.
  • Table 7 Position Intensity 1621.36 12.21 1329.64 8.292 1271.06 7.127 845.6 6.976 2930.54 6.653 1514.53 6.52 730.17 6.452 243.72 4.6 1665 4.088 335.71 4.041 3083.93 3.886 112.52 3.863 1419.75 3.709 157.14 3.505 1646.24 3.466 3050.99 3.398 891.3 3.338 1436.11 3.31 1247.4 3.287 592.4 3.169 223.76 2.857 1555.17 2.767 1234.46 2.387 2898.85 2.383 870.16 2.174 360.9 2.162 575 2.148 276.76 2.121 1092.56 2.09 1459.18 2.011 512.63 1.994 675.27 1.98 1044.27 1.823 764.63 1.748 1081.74 1.712 1383.55 1.625 973.92 1.5
  • Figure 9 shows an illustrative Raman spectrum of Form A.
  • Figure 10 shows an illustrative Raman spectrum of Form B.
  • DVS was carried out on a Surface Measurement Systems DVS 1 (S/N 990909, Balance #81317) operating under DVS Win version 2.18 and Windows 2000 software.
  • the system was previously calibrated using known relative humidity generated by saturated salt solutions at 11.8%, 33.1% and 75% relative humidity (RH). Two scans were done at 25°C from 0-90-0% RH with a step size of 10% RH and a dm/dt of 0.005. Quartz sample pans were used for all analyses.
  • Figure 11 shows an illustrative DVS of Form A.
  • Figure 12 shows an illustrative DVS of Form B.
  • Figure 13 shows an illustrative DVS of Form C.
  • the present invention is further directed to pharmaceutical compositions comprising the crystalline form of Compound 1.
  • the pharmaceutical composition comprises Form A and (ii) one or more pharmaceutically acceptable carriers and/or diluents and/or adjuvants (collectively referred to herein as "excipients") and, optionally, (iii) one or more active ingredients other than Compound 1.
  • composition essentially the entire amount of Compound 1 contained in the composition is present as substantially phase pure Form A.
  • At least a detectable fraction of Compound 1 is present in the form of Form A.
  • At least fifty percent (50%) of Compound 1 is present in the form of Form A.
  • At least ninety percent (90%) of Compound 1 is present in the form of Form A.
  • a pharmaceutical composition comprising 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide and one or more pharmaceutically acceptable excipients, wherein a detectable amount of the 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide is present as Form A crystalline 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide, wherein Form A has a melting point in a range from about 138.5 °C to about 142.5 °C, and an X-ray powder diffraction pattern comprising 3-[5
  • the pharmaceutical composition comprises Form B and (ii) one or more pharmaceutically acceptable carriers and/or diluents and/or adjuvants (collectively referred to herein as "excipients") and, optionally, (iii) one or more active ingredients other than Compound 1.
  • composition in another embodiment, essentially the entire amount of Compound 1 contained in the composition is present as substantially phase pure Form B.
  • At least a detectable fraction of Compound 1 is present in the form of Form B.
  • At least fifty percent (50%) of Compound 1 is present in the form of Form B.
  • At least ninety percent (90%) of Compound 1 is present in the form of Form B.
  • a pharmaceutical composition comprising 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide and one or more pharmaceutically acceptable excipients, wherein a detectable amount of the 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide is present as Form B crystalline 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1 (6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide, wherein Form B has a dehydration point prior to 120°C, and an X-ray powder diffraction pattern comprising peaks at 11.8 ⁇ 0.2, 15.
  • the compound of the present invention can be administered to the subject as the neat compound alone.
  • the compounds of the present invention can be presented with one or more pharmaceutically acceptable excipients in the form of a pharmaceutical composition.
  • a useful excipient can be, for example, a carrier.
  • the carrier must, of course, be acceptable in the sense of being compatible with the other ingredients of the composition and must not be deleterious to the recipient.
  • the carrier can be a solid or a liquid, or both, and is preferably formulated with the compound as a unit-dose composition, for example, a tablet, which can contain from 0.05% to 95% by weight of the active compound.
  • Other pharmacologically active substances can also be present, including other compounds of the present invention.
  • the pharmaceutical compositions of the invention can be prepared by any of the well known techniques of pharmacy, consisting essentially of admixing the components.
  • These compounds can be administered by any conventional means available for use in conjunction with pharmaceuticals, either as individual therapeutic compounds or as a combination of therapeutic compounds.
  • the amount of compound which is required to achieve the desired biological effect will, of course, depend on a number of factors such as the specific compound chosen, the use for which it is intended, the mode of administration, and the clinical condition of the recipient.
  • compositions of the invention generally can be presented in a dosage form containing about 0.1 mg to about 1000 mg of the crystalline form of Compound 1.
  • the dosage form contains about 0.1 mg to about 500 mg, 0.2 mg to about 600 mg, about 0.3 mg to about 250 mg, about 0.4 mg to about 150 mg, about 0.5 mg to about 100 mg, about 1mg to about 100 mg, about 0.6 mg to about 50 mg, about 0.7 mg to about 25 mg, about 0.8 mg to about 15 mg, about 0.9 mg to about 10 mg, or about 1 mg to about 5 mg of the crystalline form of Compound 1.
  • the dosage form contains less than about 100 mg, less than about 75 mg, less than about 50 mg, less than about 25 mg, or less than about 10 mg of the crystalline form of Compound 1.
  • This total daily dose can be administered to the patient in a single dose, or in proportionate multiple subdoses. Subdoses can be administered 2 to 6 times per day. Doses can be in sustained release form effective to obtain desired results.
  • Illustrative non-limiting dosage unit forms of the pharmaceutical compositions can typically contain, for example, 0.1, 0.2, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9 10, 20, 25, 30, 37.5, 40, 50, 75, 100, 125, 150, 175, 200, 250, 300, 350 or 400 mg of the crystalline form of Compound 1.
  • Oral delivery of the compound of the present invention can include formulations, as are well known in the art, to provide prolonged or sustained delivery of the drug to the gastrointestinal tract by any number of mechanisms. These include, but are not limited to, pH sensitive release from the dosage form based on the changing pH of the small intestine, slow erosion of a tablet or capsule, retention in the stomach based on the physical properties of the formulation, bioadhesion of the dosage form to the mucosal lining of the intestinal tract, or enzymatic release of the active drug from the dosage form. The intended effect is to extend the time period over which the active drug molecule is delivered to the site of action by manipulation of the dosage form.
  • enteric-coated and enteric- coated controlled release formulations are within the scope of the present invention. Suitable enteric coatings include cellulose acetate phthalate, polyvinylacetate phthalate, hydroxypropylmethylcellulose phthalate and anionic polymers of methacrylic acid and methacrylic acid methyl ester.
  • the daily dose can, for example, be in the range of from about 0.1 mg/kg body weight to about 20 mg/kg body weight, preferably from about 0.25 mg/kg body weight to about 10 mg/kg body weight, more preferably from about 0.4 mg/kg body weight to about 5 mg/kg body weight.
  • This dose can be conveniently administered as an infusion of from about 10 ng/kg body weight to about 2000 ng/kg body weight per minute.
  • Infusion fluids suitable for this purpose can contain, for example, from about 0.1 ng to about 10 mg, preferably from about 1 ng to about 200 mg per milliliter.
  • Unit doses can contain, for example, from about 1 mg to about 200 g of the compound of the present invention.
  • ampoules for injection can contain, for example, from about 1 mg to about 200 mg.
  • compositions according to the present invention include those suitable for oral, rectal, topical, buccal (e.g., sublingual), and parenteral (e.g., subcutaneous, intramuscular, intradermal, or intravenous) administration, although the most suitable route in any given case will depend on the nature and severity of the condition being treated and on the nature of the particular compound which is being used. In most cases, the preferred route of administration is oral.
  • Formulations suitable for topical administration to the eye also include eye drops wherein the active ingredients are dissolved or suspended in suitable carrier, especially an aqueous solvent for the active ingredients.
  • suitable carrier especially an aqueous solvent for the active ingredients.
  • the anti-inflammatory active ingredients are preferably present in such formulations in a concentration of 0.5 to 20%, advantageously 0.5 to 10% and particularly about 1.5% w/w.
  • compositions suitable for oral administration can be presented in discrete units, such as capsules, cachets, lozenges, or tablets, each containing a predetermined amount of at least one compound of the present invention; as a powder or granules; as a solution or a suspension in an aqueous or non-aqueous liquid; or as an oil-in-water or water-in-oil emulsion.
  • such compositions can be prepared by any suitable method of pharmacy which includes the step of bringing into association the active compound(s) and the carrier (which can constitute one or more accessory ingredients).
  • the compositions are prepared by uniformly and intimately admixing the active compound with a liquid or finely divided solid carrier, or both, and then, if necessary, shaping the product.
  • a tablet can be prepared by compressing or molding a powder or granules of the compound, optionally with one or more assessory ingredients.
  • Compressed tablets can be prepared by compressing, in a suitable machine, the compound in a free-flowing form, such as a powder or granules optionally mixed with a binder, lubricant, inert diluent and/or surface active/dispersing agent(s).
  • Molded tablets can be made by molding, in a suitable machine, the powdered compound moistened with an inert liquid diluent.
  • compositions suitable for buccal (sub-lingual) administration include lozenges comprising a compound of the present invention in a flavored base, usually sucrose, and acacia or tragacanth, and pastilles comprising the compound in an inert base such as gelatin and glycerin or sucrose and acacia.
  • compositions suitable for parenteral administration conveniently comprise sterile aqueous preparations of a compound of the present invention. These preparations are preferably administered intravenously, although administration can also be effected by means of subcutaneous, intramuscular, or intradermal injection. Such preparations can conveniently be prepared by admixing the compound with water and rendering the resulting solution sterile and isotonic with the blood. Injectable compositions according to the invention will generally contain from 0.1 to 5% w/w of a compound disclosed herein.
  • compositions suitable for rectal administration are preferably presented as unit-dose suppositories. These can be prepared by admixing a compound of the present invention with one or more conventional solid carriers, for example, cocoa butter, and then shaping the resulting mixture.
  • compositions suitable for topical application to the skin preferably take the form of an ointment, cream, lotion, paste, gel, spray, aerosol, or oil.
  • Carriers which can be used include vaseline, lanoline, polyethylene glycols, alcohols, and combinations of two or more thereof.
  • the active compound is generally present at a concentration of from 0.1 to 15% w/w of the composition, for example, from 0.5 to 2%.
  • compositions suitable for transdermal administration can be presented as discrete patches adapted to remain in intimate contact with the epidermis of the recipient for a prolonged period of time.
  • patches suitably contain a compound of the present invention in an optionally buffered, aqueous solution, dissolved and/or dispersed in an adhesive, or dispersed in a polymer.
  • a suitable concentration of the active compound is about 1% to 35%, preferably about 3% to 15%.
  • the compound can be delivered from the patch by electrotransport or iontophoresis, for example, as described in Pharmaceutical Research, 3(6), 318 (1986).
  • the amount of active ingredient that can be combined with carrier materials to produce a single dosage form to be administered will vary depending upon the host treated and the particular mode of administration.
  • the solid dosage forms for oral administration including capsules, tablets, pills, powders, and granules noted above comprise one or more compounds of the present invention admixed with at least one inert diluent such as sucrose, lactose, or starch.
  • Such dosage forms may also comprise, as in normal practice, additional substances other than inert diluents, e.g., lubricating agents such as magnesium stearate.
  • the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings.
  • Liquid dosage forms for oral administration can include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs containing inert diluents commonly used in the art, such as water.
  • Such compositions may also comprise adjuvants, such as wetting agents, emulsifying and suspending agents, and sweetening, flavoring, and perfuming agents.
  • sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or setting agents and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol.
  • acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil may be employed including synthetic mono- or diglycerides.
  • fatty acids such as oleic acid find use in the preparation of injectables.
  • compositions encompass all the foregoing and the like.
  • the present invention also embraces a method for treatment and/or prophylaxis of a p38 kinase-mediated condition, the method comprising treating a subject having or susceptible to such condition or disorder with a therapeutically effective amount of a solid-state form of Compound 1 or a pharmaceutical composition containing a solid-state form of Compound 1.
  • the p38 kinase-mediated condition is rheumatoid arthritis.
  • Such a method is useful for treatment and/or prophylaxis of a condition in a subject where administration of a p38 kinase inhibitor is indicated, including, but not limited to, treatment of those conditions previously disclosed above.
  • Solid-state forms of Compound 1 and pharmaceutical compositions thereof are also useful for veterinary treatment of companion, exotic and farm animals, for example horses, dogs, and cats.
  • the solid-state forms of Compound 1 and compositions thereof also can be used (i) in therapies partially or completely in place of other anti-inflammatory drugs, and/or (ii) in combination therapies with other drugs.
  • anti-inflammatory and other drugs may include, but are not limited to, steroids, cyclooxygenase-2 inhibitors, DMARD's, immunosuppressive agents, NSAIDs, 5-lipoxygenase inhibitors, LTB 4 antagonists and LTA 4 hydrolase inhibitors.
  • phrase "combination therapy” embraces administration of each drug in a sequential manner in a regimen that will provide beneficial effects of the drug combination, as well as co-administration of the drugs in a substantially simultaneous manner, such as in a single capsule or injection having a fixed ratio of these active agents or in multiple, separate dosage forms or injections, one for each agent.
  • Form A was prepared by dissolving 34 mg of amorphous 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide in 0.5 ml of methyl ethyl ketone. The mixture was allowed to air dry in a hood resulting in Form A.
  • Form A can also be prepared by the recrystallization from methyl t-butyl ether. 35 mg amorphous 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide is dissolved in 0.25 ml methyl t-butyl ether. The solution is allowed to stand and the resulting precipitate is filtered and air dried resulting in Form A.
  • Form A can also be prepared by slurrying 34 mg of amorphous 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide in 0.5ml isopropyl ether. The resulting solid is filtered and air dried resulting in Form A
  • Form A can also be prepared by direct crystallization of amorphous 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydioxyethyl)-4-methylbenzamide in methyl ethyl ketone. 100 mg of 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide is dissolved in 1ml of MEK. Upon recrystallization the material is filtered and air dried resulting in Form A.
  • Form A can also be prepared by slurry from the following solvents: ethanol, dioxane, tetrahydro furan, and dimethyl formamide.
  • Form B was prepared by the slurry of 185 mg of amorphous 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide in 3 ml of water for 7 days. The solid material was filtered and air dried resulting in Form B.
  • Form B can also be prepared by slurrying amorphous 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide or crystalline Form A in ethanol and water mixtures with a water activity of 0.4 and above.
  • Form C was prepared by slurrying 31 mg of amorphous 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide in 1 ml of water. The resulting solid was filtered and air dried.

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EP13186682.4A 2004-10-13 2005-10-03 Formes Cristallines De 3-[5-Chloro-4-(2,4-difluorobenzyl) oxy]-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide Withdrawn EP2708531A1 (fr)

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US61846604P 2004-10-13 2004-10-13
EP05787468.7A EP1802589B1 (fr) 2004-10-13 2005-10-03 Formes cristallines de 3-[5-chloro-4-(2,4-difluorobenzyl) oxy]-6-oxopyrimidin-1(6h)-yl]-n-(2-hydroxyethyl)-4-methylbenzamide

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EP05787468.7A Division-Into EP1802589B1 (fr) 2004-10-13 2005-10-03 Formes cristallines de 3-[5-chloro-4-(2,4-difluorobenzyl) oxy]-6-oxopyrimidin-1(6h)-yl]-n-(2-hydroxyethyl)-4-methylbenzamide

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FR2849029B1 (fr) 2002-12-20 2005-03-18 Lafon Labor Procede de preparation et formes cristallines des enantiomeres optiques du modafinil.
EP1992344A1 (fr) 2007-05-18 2008-11-19 Institut Curie P38 alpha comme cible therapeutique pour les maladies associées á une mutation de FGFR3
CA2750565C (fr) * 2009-01-30 2015-10-20 Glaxosmithkline Llc Chlorhydrate de n-{(1-s)-2-amino-1-[(3-fluorophenyl)methyl]ethyl}-5-chloro-4-(4-chloro-1-methyl-1h-pyrazol-5-yl)-2-thiophenecarboxamide cristallin
RS54978B1 (sr) 2009-11-27 2016-11-30 Genzyme Corp Genz 112638 za lečenje gošeove ili fabrijeve bolesti u kombinacionoj terapiji
KR20140053836A (ko) 2011-01-11 2014-05-08 글락소스미스클라인 엘엘씨 조합물
KR101252711B1 (ko) * 2011-03-31 2013-04-09 김두철 가구용 경첩
CN103570630B (zh) * 2012-07-18 2016-04-20 广东东阳光药业有限公司 氮杂环衍生物及其在药物中的应用
EP3083584B1 (fr) 2013-12-19 2018-02-21 Sunshine Lake Pharma Co., Ltd. Dérivés hétérocycliques azotés et leur application dans des médicaments pour le traitement de la fibrose tissulaire

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999064400A1 (fr) * 1998-06-12 1999-12-16 Vertex Pharmaceuticals Incorporated INHIBITEURS DE p38
WO2001029010A1 (fr) * 1999-10-21 2001-04-26 Merck & Co., Inc. Composes antibacteriens a selectivite gram-positif, compositions contenant ces composes et methodes therapeutiques
WO2004087677A2 (fr) * 2003-04-03 2004-10-14 Pharmacia Corporation Pyrimidinones substituees

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61205261A (ja) 1985-03-08 1986-09-11 Sagami Chem Res Center ６―置換―５―フルオロウラシル誘導体
JPH09504010A (ja) 1993-10-20 1997-04-22 ジ・アップジョン・カンパニー 抗関節炎剤および抗炎症剤としてのピリミジノン
HUP0001140A3 (en) 1996-12-05 2002-05-28 Amgen Inc Thousand Oaks Substituted pyrimidinone and pyridone compounds and methods of use
EP1553949B1 (fr) 2002-08-13 2007-04-18 Warner-Lambert Company LLC Derives de pyrimidine 2,4-diones, utilises comme inhibiteurs de metalloproteinase matricielle
US20070167621A1 (en) * 2003-04-03 2007-07-19 Pharmacia Corporation Substituted pyrimidinones

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999064400A1 (fr) * 1998-06-12 1999-12-16 Vertex Pharmaceuticals Incorporated INHIBITEURS DE p38
WO2001029010A1 (fr) * 1999-10-21 2001-04-26 Merck & Co., Inc. Composes antibacteriens a selectivite gram-positif, compositions contenant ces composes et methodes therapeutiques
WO2004087677A2 (fr) * 2003-04-03 2004-10-14 Pharmacia Corporation Pyrimidinones substituees

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
GOLDNER H ET AL: "EINE NEUE XANTHIN-SYNTHESE", JUSTUS LIEBIGS ANNALEN DER CHEMIE, VERLAG CHEMIE, WEINHEIM,, DE, vol. 691, 1966, pages 142 - 158, XP002294077, ISSN: 0075-4617 *
WHITEHEAD C W ET AL: "Exchange amination. Alkyl- and arylaminopyrimidines and purines", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, US, vol. 82, 1960, pages 3971 - 3974, XP002294078, ISSN: 0002-7863 *

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ZA200701999B (en) 2008-10-29
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IL181815A0 (en) 2007-07-04
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WO2006040649A1 (fr) 2006-04-20
EP1802589B1 (fr) 2014-04-09
TW200626562A (en) 2006-08-01
US8324230B2 (en) 2012-12-04
AU2005293290A1 (en) 2006-04-20
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KR20070083663A (ko) 2007-08-24
US20080269264A1 (en) 2008-10-30

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